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M. Génévriez

Publications and source records attributed to M. Génévriez.

2 recordsLinked to original sources

High-Resolution Spectroscopy of the X-A Transition of the Carbon Monoxide Dication CO$^{2+}$

We report rovibronic spectra of the A $^3Σ^+$($v'=0-2$) - X $^3Π_Ω(v=0)$ rovibronic transitions ($|Ω|=0, 1$ and 2) of the CO$^{2+}$ doubly-charged molecular ion. Spectra were recorded at high resolution ($\sim 5$~cm$^{-1}$) in a fast beam of CO$^{2+}$ molecules by detecting the Coulomb explosion of the molecules upon excitation to the A state. Measurements were guided by \textit{ab initio} calculations which then assisted the assignment of the observed spectral features. Our results resolve the spin-orbit splittings of the ground vibronic state X $^3Π_Ω(v=0)$, but not the rotational structure of the bands due to spectral congestion, and provide spectroscopic information on CO$^{2+}$ with unprecedented resolution. In doing so they expand our knowledge of this benchmark doubly charged molecular ion and expand the short list of doubly charged molecules studied at high resolution.

physics.atom-ph↗

Isolated-core quadrupole excitation of highly excited autoionizing Rydberg states

The structure and photoexcitation dynamics of high lying doubly excited states of the strontium atom with high angular momenta are studied in the vicinity of the Sr$^+(N=5)$ threshold. The spectra recorded using resonant multiphoton isolated core excitation are analyzed with calculations based on configuration interaction with exterior complex scaling, which treats the correlated motion of the two valence electrons of Sr from first principles. The results are rationalized with a model based on multichannel quantum-defect theory and transition dipole moments calculated with a perturbative treatment of electron correlations. Together, both approaches reveal that most of the lines observed in the spectra arise from the interaction of a single optically active state, coupled to the initial state by an electric-dipole transition, with entire doubly-excited Rydberg series. The long-range electron correlations responsible for this interaction unexpectedly vanish for identical values of the initial and final principal quantum numbers, a fact related to the quasi hydrogenic nature of the high-$l$ Rydberg electron. This special situation, and in particular the vanishing interaction, leads to the surprising observation of an electric \emph{quadrupole} isolated-core excitation with a similar intensity as the neighboring electric dipole transitions.

physics.atom-ph↗